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CAS 32233-43-5

(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane TCI H1189

(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane TCI H1189

Chemical Identity

CAS No.
32233-43-5
PubChem
CID 11051805·SID 87560258
Formula
C7H14O3
Molecular weight
146.18 g/mol
Purity
>95.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol
SMILES
CC1(OC[C@@H](O1)CCO)C
InChIKey
YYEZYENJAMOWHW-LURJTMIESA-N
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(S)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. This material plays a crucial role in the laboratory by serving as a chiral building block, enabling the synthesis of enantiomerically pure compounds. Its application is essential in the development of bioactive compounds, including pharmaceuticals and pharmacological agents. Due to its stability and reactivity, it is a preferred choice for various chemical reactions. The chiral nature of this compound allows for the formation of different isomers, which is vital in asymmetric synthesis. This property makes it ideal for reactions requiring precise control over molecular structure. Additionally, its good solubility in organic solvents facilitates processing and chemical reactions. In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in educational institutions and research centers focused on synthetic chemistry.

  • Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds due to its chiral structure, which allows for precise control over stereochemistry.
  • Pharmaceutical Development: It is used in the synthesis of bioactive molecules, including drugs and pharmacological agents, where stereochemical purity is critical.
  • Organic Chemistry Research: Its stability and solubility make it a valuable tool for synthetic pathways in academic and industrial research settings.
  • Chiral Catalyst Studies: It serves as a building block for developing and testing chiral catalysts in asymmetric reactions.
  • Structural Analysis: It is used in analytical chemistry for studying the properties and behavior of chiral compounds in various reaction conditions.

Brand TCI
CAS number 32233-43-5
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various sizes as per standard chemical supply practices
Physical form Liquid
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its chiral nature, it is important to handle it with care to avoid any unintended isomer formation during synthesis. In laboratory settings, proper ventilation and personal protective equipment should be used when handling this compound to ensure safety. It is also advisable to keep it away from incompatible substances to prevent any chemical reactions that could compromise its integrity.

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